FDA.reportPublic FDA data

BURTON

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30001316313000131631Burton Corporation1Y2026-01-01180 Queen City Park Rd Burlington VT US 05401
30095429563009542956Burton Medical LLC1N2026-01-012300 W Windsor Ct. STE C Addison IL US 60101
30148337973014833797BURTON DENTAL INNOVATIONS, LLC1N2020-04-25607 S Adams St Hinsdale IL US 60521

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
1408402072961684K963682GENIE' SINGLE CEILING AND DOUBLE CEILINGFSY1996-11-13
1408401399433685K101537AIM 200, MAJOR SURGICAL LIGHTFSY2010-09-30
1408401793881378K042395OUTPATIENT III MINOR SURGERY LIGHTFSY2004-12-01
2220601281438368
1408401050856267
1408401142077389
1408401197709457
1408401283219281

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
FSY32010-09-30

PMN#

GENIE

1996-08-22

BURTON MEDICAL PRODUCTS CORP.

GENESIS

1994-06-23

BURTON MEDICAL PRODUCTS CORP.

GUDID#